Cannula insertion devices, systems, and methods including a compressible member

• US 8,333,686 B2
• Filed: 08/29/2007
• Issued: 12/18/2012
• Est. Priority Date: 08/30/2006
• Status: Active Grant

• Current Assignee: Circulite Inc. (Medtronic Plc)
• Original Assignee: Circulite Inc. (Medtronic Plc)
• Inventors: Marseille, Oliver, Kerkhoffs, Wolfgang
• Primary Examiner(s): Layno, Carl H.
• Assistant Examiner(s): MORALES, JON ERIC C
• Application Number:
  US11/846,886
• Publication Number:
  US 20080076960A1
• Time in Patent Office: 1,938 Days
• Field of Search: 600/16
• US Class Current: 600/16
• CPC Class Codes: A61B 17/3415 for introducing tubes or catheters, e.g. gastrostomy tubes, drain catheters A61B17/3417 takes precedence; body piercing catheter guide needles A61M25/06
• CPC Class Codes: A61M 25/04 in the body, e.g. expansible A61M25/10, A61M16/0488 take precedence
• CPC Class Codes: A61M 25/0662 Guide tubes
• CPC Class Codes: A61M 60/122 Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body
• CPC Class Codes: A61M 60/148 in line with a blood vessel using resection or like techniques, e.g. permanent endovascular heart assist devices
• CPC Class Codes: A61M 60/20 Type thereof
• CPC Class Codes: A61M 60/857 Implantable blood tubes
• CPC Class Codes: A61M 60/861 Connections or anchorings for connecting or anchoring pumps or pumping devices to parts of the patient's body
• CPC Class Codes: A61M 60/865 Devices for guiding or inserting pumps or pumping devices into the patient's body

Abstract

An insertion device for inserting a cannula through tissue generally comprises an inner shaft, a tip member coupled to a distal end portion of the inner shaft, a hollow outer shaft slidably received over the inner shaft, and a compressible member received over the inner shaft between the tip member and the outer shaft. The compressible member is configured to be received in a lumen of the cannula, and the inner shaft is movable relative to the outer shaft along an axial direction to compress the compressible member between the tip member and the outer shaft so that the compressible member expands in a generally radially outward direction. The radial expansion of the compressible member releasably secures the insertion device to the cannula.

Claims

1. A cannula assembly, comprising:

a cannula having an inner wall defining a lumen; and

an insertion device including;

(a) a shaft including a distal end, the shaft configured to be received within the lumen of the cannula;

(b) a tip member coupled to the distal end of the shaft, the tip member configured to extend distally out from the lumen of the cannula so as to be in position for dilating a puncture in a tissue;

(c) a compressible member operatively coupled to the shaft and configured to expand in a generally radially outward direction when compressed in an axial direction;

wherein the compressible member is movable from an initial state in which the compressible member has a first radial dimension to a compressed state in which the compressible member has a second radial dimension that is larger than the first radial dimension, the second radial dimension configured to engage the inner wall of the lumen of the cannula to releasably secure the insertion device to the cannula.

2. A method of inserting a cannula through tissue, the cannula including a lumen and a distal end portion, the method comprising:

inserting an insertion device including a distal connecting portion into the lumen of the cannula wherein the distal connecting portion comprises an inner shaft having a distal end, a tip member coupled to the distal end of the inner shaft, and a compressible member operably coupled to the inner shaft;

compressing the compressible member of the insertion device in an axial direction to expand the compressible member in a generally radially outward direction so as to connect the distal connecting portion of the insertion device to the distal end portion of the cannula; and

inserting the distal end portion of the cannula through the tissue while the distal connecting portion is connected to the distal end portion by exerting a pushing force on the insertion device.

3. The method of claim 2 wherein the tissue defines a wall of a chamber of a heart, and wherein inserting the distal end portion of the cannula through the tissue comprises inserting the distal end portion of the cannula into the chamber of the heart.

4. The method of claim 2, further comprising:

securing the cannula to the tissue;

radially contracting the compressible member to release the distal connecting portion of the insertion device from the distal end portion of the cannula; and

removing the insertion device from the cannula.

5. The method of claim 2, the insertion device further comprising a hollow outer shaft slidably positioned over the inner shaft, the compressible member being received on the inner shaft between the hollow outer shaft and the tip member, and wherein compressing the compressible member further comprises:

moving the inner shaft relative to the hollow outer shaft along the axial direction so that the compressible member is compressed between the hollow outer shaft and the tip member.

6. The method of claim 5 wherein moving the inner shaft relative to the hollow outer shaft further comprises:

manipulating a handle member associated with the inner shaft.

7. The method of claim 2 wherein compressing the compressible member causes the compressible member to exert a radial force against an inner wall of the cannula and to form a seal between the distal connecting portion of the insertion device and the distal end portion of the cannula, the method further comprising:

radially contracting the compressible member an initial amount to reduce the radial force applied by the compressible member against the cannula, wherein the compressible member maintains the seal between the insertion device and the cannula when radially contracted the initial amount; and

retracting the distal connecting portion of the insertion device at least partially through the lumen of the cannula.

8. The method of claim 7 wherein the distal connecting portion engages the cannula at a first portion of the lumen and retracting the insertion device moves the distal connecting portion from the first portion of the lumen to a second portion of the lumen so as to draw blood into the first portion of the lumen, the method further comprising:

forming a seal between the first portion of the cannula and a second portion of the cannula, the second portion being at least partially occupied by the distal connecting portion of the insertion device after retracting the distal connecting portion; and

removing the insertion device from the cannula after forming the seal.

9. The method of claim 8, further comprising:

radially contracting the compressible member an additional amount before removing the insertion device from the cannula to release the distal connecting portion from the second portion of the cannula.

10. The method of claim 9, further comprising:

coupling the cannula to an inlet of a blood pump; and

releasing the seal formed between the first portion and second portion of the cannula.

11. A system for increasing blood flow between a chamber in a heart of a patient and a first location in the circulatory system of the patient remote from the chamber, the system comprising:

a blood pump having an inlet and an outlet, the outlet being adapted for connection to the first location in the circulatory system of the patient;

a cannula having an inner wall defining a lumen, a proximal end portion configured to couple to the inlet of the blood pump, and a distal end portion configured for insertion into the chamber of the heart; and

an insertion device for assisting with insertion of the distal end of the cannula into the chamber of the heart, including

a shaft including a distal end, the shaft configured to be received within the lumen of the cannula;

a tip member coupled to the distal end of the shaft, the tip member configured to extend distally out from the lumen of the cannula so as to be in position for dilating a puncture in the tissue; and

a compressible member operatively coupled to the shaft and configured to expand in a generally radially outward direction when compressed in an axial direction;

wherein the compressible member is movable from an initial state in which the compressible member has a first radial dimension to a compressed state in which the compressible member has a second radial dimension that is larger than the first radial dimension, the second radial dimension configured to engage the inner wall of the lumen of the cannula to releasably secure the insertion device to the cannula.